Data / Medical devices / Calibrator, Volume, Gas
Calibrator, Volume, Gas (BXW): 9 FDA-registered makers in 5 countries
9 establishments in 5 countries are registered with the FDA to make Calibrator, Volume, Gas (product code BXW, Class 1, 21 CFR 868.1870). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 6 510(k) clearances under this code, the latest on December 5, 1985, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- BXW
- Device class
- 1
- Regulation
- 868.1870
- Medical specialty
- Anesthesiology
Makers by country
| Country | Makers |
|---|---|
| United States | 4 |
| Germany | 2 |
| Taiwan | 1 |
| China | 1 |
| Ireland | 1 |
Makers of Calibrator, Volume, Gas
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| A-M Systems | Sequim, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Aspen Surgical Products, Inc. | Caledonia, MI, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Allied Medical LLC | Earth City, MO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Besmed Health Business Corporation | New Taipei City, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Englert GMBH & Co. KG | Wertheim Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hans Rudolph, Inc. | Shawnee, KS, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jaeger Medical GmbH | HOECHBERG Bavaria, Germany | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shandong Jinlai Huanhai Medical Technology Co.,ltd | Yantai Shandong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vitalograph Ireland Ltd. | Co Clare, Ireland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated December 5, 1985. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.